510(k) K862656 ยท DTD Pacemaker Lead Adaptor
PACEMAKER LEAD ADAPTER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jul 30, 1986 |
| Received | Jul 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862656
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.